[Federal Register Volume 60, Number 235 (Thursday, December 7, 1995)]
[Notices]
[Pages 62869-62870]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 95-29808]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
[Docket No. 95E-0302]
Determination of Regulatory Review Period for Purposes of Patent
Extension; ULTANETM
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice.
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SUMMARY: The Food and Drug Administration (FDA) has determined the
regulatory review period for ULTANETM and is publishing this
notice of that determination as required by law. FDA has made the
determination because of the submission of an application to the
Commissioner of Patents and Trademarks, Department of Commerce, for the
extension of a patent which claims that human drug product.
ADDRESSES: Written comments and petitions should be directed to the
Dockets Management Branch (HFA-305), Food and Drug Administration, rm.
1-23, 12420 Parklawn Dr., Rockville, MD 20857.
FOR FURTHER INFORMATION CONTACT: Brain J. Malkin, Office of Health
Affairs (HFY-20), Food and Drug Administration, 5600 Fishers Lane,
Rockville, MD 20857, 301-443-1382.
SUPPLEMENTARY INFORMATION: The Drug Price Competition and Patent Term
Restoration Act of 1984 (Pub. L. 98-417) and the Generic Animal Drug
and Patent Term Restoration Act (Pub. L. 100-670) generally provide
that a patent may be extended for a period of up to 5 years so long as
the patented item (human drug product, animal drug product, medical
device, food additive, or color additive) was subject to regulatory
review by FDA before the item was marketed. Under these acts, a
product's regulatory review period forms the basis for determining the
amount of extension an applicant may receive.
A regulatory review period consists of two periods of time: A
testing phase and an approval phase. For human drug products, the
testing phase begins when the exemption to permit the clinical
investigations of the drug becomes effective and runs until the
approval phase begins. The approval phase starts with the initial
submission of an application to market the human drug product and
continues until FDA grants permission to market the drug product.
Although only a portion of a regulatory review period may count toward
the actual amount of extension that the Commissioner of Patents and
Trademarks may award (for example, half the testing phase must be
subtracted as well as any time that may have occurred before the patent
was issued), FDA's determination of the length of a regulatory review
period for a human drug product will include all of the testing phase
and approval phase as specified in 35 U.S.C. 156(g)(1)(B).
FDA recently approved for marketing the human drug product
ULTANETM (sevoflurane). ULTANETM is indicated for induction
and maintenance of general anesthesia in adult and pediatric patients
for inpatient and outpatient surgery. Subsequent to this approval, the
Patent and Trademark Office received a patent term restoration
application for ULTANETM (U.S. Patent No. 4,250,334) from Baxter
International, Inc., and the Patent and Trademark Office requested
FDA's assistance in determining this patent's eligibility for patent
term restoration. In a letter dated September 25, 1995, FDA advised the
Patent and Trademark Office that this human drug product had undergone
a regulatory review period and that the approval of ULTANETM
represented the first permitted commercial marketing or use of the
product. Shortly thereafter, the Patent and Trademark Office requested
that FDA determine the product's regulatory review period.
FDA has determined that the applicable regulatory review period for
ULTANETM is 3,418 days. Of this time, 3,086 days occurred during
the testing phase of the regulatory review period, while 332 days
occurred during the approval phase. These periods of time were derived
from the following dates:
1. The date an exemption under section 505(i) of the Federal Food,
Drug, and Cosmetic Act (21 U.S.C. 355(i)) became effective: January 29,
1986. The applicant claims January 10, 1986, as the date the
investigational new drug (IND) became effective. However, FDA records
indicate that the correct IND effective date was January 29, 1985,
which was 30 days after FDA receipt of IND 27,645 on December 30, 1985.
2. The date the application was initially submitted with respect to
the human drug product under section 505(b) of the Federal Food, Drug,
and Cosmetic Act: July 11, 1994. The applicant claims July 8, 1994, as
the date the new drug application (NDA) for ULTANETM (NDA 20-478)
was initially submitted. However, FDA records indicate that the
applicant submitted NDA 20-478 on July 8, 1994, and the agency received
the NDA on July 11, 1994, which is considered to be the NDA initially
submitted date.
3. The date the application was approved: June 7, 1995. FDA has
verified the applicant's claim that NDA 20-478 was approved on June 7,
1995.
This determination of the regulatory review period establishes the
maximum potential length of a patent extension. However, the U.S.
Patent and Trademark Office applies several statutory limitations in
its calculations of the actual period for patent extension. In its
application for patent extension, this applicant seeks 1,826 days of
patent term extension.
Anyone with knowledge that any of the dates as published is
incorrect may, on or before February 5, 1996, submit to the Dockets
Management Branch (address above) written comments and ask for a
redetermination. Furthermore,
[[Page 62870]]
any interested person may petition FDA, on or before June 5, 1996, for
a determination regarding whether the applicant for extension acted
with due diligence during the regulatory review period. To meet its
burden, the petition must contain sufficient facts to merit an FDA
investigation. (See H. Rept. 857, part 1, 98th Cong., 2d sess., pp. 41-
42, 1984.) Petitions should be in the format specified in 21 CFR 10.30.
Comments and petitions should be submitted to the Dockets
Management Branch (address above) in three copies (except that
individuals may submit single copies) and identified with the docket
number found in brackets in the heading of this document. Comments and
petitions may be seen in the Dockets Management Branch between 9 a.m.
and 4 p.m., Monday through Friday.
Dated: November 30, 1995.
Stuart L. Nightingale,
Associate Commissioner for Health Affairs.
[FR Doc. 95-29808 Filed 12-6-95; 8:45 am]
BILLING CODE 4160-01-F
